Hydroxyurea to prevent brain injury in children with sickle cell disease (HU Prevent)-A randomized, placebo-controlled phase II feasibility/pilot study

被引:4
作者
Casella, James F. [1 ]
Furstenau, Dana K. [1 ]
Adams, Robert J. [2 ]
Brambilla, Donald J. [3 ]
Lebensburger, Jeffrey D. [4 ]
Fehr, James J. [5 ]
Jordan, Lori C. [6 ]
King, Allison A. [7 ,8 ]
Ichord, Rebecca N. [9 ]
McKinstry, Robert C. [10 ]
Kraut, Michael A. [11 ]
Shaw, Dennis W. [12 ]
White, Desiree A. [13 ]
Whyte-Stewart, Donna A. [14 ]
Avadhani, Radhika [15 ]
Barron-Casella, Emily A. [1 ]
Cannon, Alicia D. [16 ]
Eaton, Cyd K. [17 ]
Riekert, Kristin A. [18 ]
Shay, Joanne E. [19 ]
Smith-Seidel, Cynthia A. [20 ]
Weiss, Diane C. [1 ]
Ostapkovich, Noeleen D. [15 ]
Vermillion, Krista [21 ]
Treine, Kevin E. [15 ]
Kingsbury, Claire E. [1 ]
Strouse, John J. [22 ]
Thompson, Richard E. [23 ]
Hanley, Daniel F. [15 ]
机构
[1] Johns Hopkins Univ, Dept Pediat, Div Hematol, Sch Med, 720 Rutland Ave,Ross Res Bldg 1125, Baltimore, MD 21205 USA
[2] Med Univ South Carolina, Dept Neurol, Charleston, SC USA
[3] Res Triangle Inst RTI Int, Rockville, MD USA
[4] Univ Alabama Birmingham, Dept Pediat, Div Pediat Hematol Oncol, Birmingham, AL USA
[5] Stanford Univ Sch Med, Dept Anesthesiol Perioperat & Pain Med, Stanford, CA USA
[6] Vanderbilt Univ, Dept Pediat, Div Pediat Neurol, Med Ctr, Nashville, TN USA
[7] Washington Univ, Div Pediat Hematol Oncol, St Louis, MO USA
[8] St Louis Childrens Hosp, St Louis, MO USA
[9] Univ Penn, Childrens Hosp Philadelphia, Perelman Sch Med, Dept Neurol & Pediat, Philadelphia, PA USA
[10] Washington Univ, Mallinckrodt Inst Radiol, Sch Med, St Louis, MO USA
[11] Johns Hopkins Univ, Dept Radiol & Radiol Sci, Sch Med, Baltimore, MD USA
[12] Seattle Childrens Hosp, Dept Radiol, Seattle, WA USA
[13] Washington Univ St Louis, Dept Psychol & Brain Sci, St Louis, MO USA
[14] Food & Drug Adm FDA, Div Nonmalignant Hematol, Silver Spring, MD USA
[15] Johns Hopkins Univ, BIOS Clin Trials Coordinating Ctr, Dept Neurol & Neurosurg, Sch Med, Baltimore, MD USA
[16] Kennedy Krieger Inst, Dept Neuropsychol, Baltimore, MD USA
[17] Johns Hopkins Bayview, Biostat Epidemiol & Data Management Core, Med Ctr, Baltimore, MD USA
[18] Johns Hopkins Univ, Dept Med, Div Pulm & Crit Care Med, Sch Med, Baltimore, MD USA
[19] Johns Hopkins Univ, Sch Med, Dept Anesthesiol & Crit Care Med, Baltimore, MD USA
[20] Martinsburg Vet Affairs Med Ctr VAMC, Dept Psychol, Martinsburg, WV USA
[21] Vanderbilt Univ, Vanderbilt Inst Clin & Translat Res VICTR, Med Ctr, Nashville, TN USA
[22] Duke Univ, Dept Med & Pediat, Sch Med, Durham, NC USA
[23] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD USA
关键词
YOUNG-CHILDREN; CONTROLLED-TRIAL; ANEMIA; TRANSFUSIONS; ASSOCIATION; MANAGEMENT; ANESTHESIA; EXPOSURE; AGE;
D O I
10.1002/ajh.27423
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Central nervous system (CNS) injury is common in sickle cell disease (SCD) and occurs early in life. Hydroxyurea is safe and efficacious for treatment of SCD, but high-quality evidence from randomized trials to estimate its neuroprotective effect is scant. HU Prevent was a randomized (1:1), double-blind, phase II feasibility/pilot trial of dose-escalated hydroxyurea vs. placebo for the primary prevention of CNS injury in children with HbSS or HbS-beta(0)-thalassemia subtypes of SCD age 12-48 months with normal neurological examination, MRI of the brain, and cerebral blood flow velocity. We hypothesized that hydroxyurea would reduce by 50% the incidence of CNS injury. Two outcomes were compared: primary-a composite of silent cerebral infarction, elevated cerebral blood flow velocity, transient ischemic attack, or stroke; secondary-a weighted score estimating the risk of suffering the consequences of stroke (the Stroke Consequences Risk Score-SCRS), based on the same outcome events. Six participants were randomized to each group. One participant in the hydroxyurea group had a primary outcome vs. four in the placebo group (incidence rate ratio [90% CI] 0.216 [0.009, 1.66], p = .2914) (similar to 80% reduction in the hydroxyurea group). The mean SCRS score was 0.078 (SD 0.174) in the hydroxyurea group, 0.312 (SD 0.174) in the placebo group, p = .072, below the p-value of .10 often used to justify subsequent phase III investigations. Serious adverse events related to study procedures occurred in 3/41 MRIs performed, all related to sedation. These results suggest that hydroxyurea may have profound neuroprotective effect in children with SCD and support a definitive phase III study to encourage the early use of hydroxyurea in all infants with SCD.
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收藏
页码:1906 / 1916
页数:11
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